Canonical Allele Identifier: CA419891379
Gene: TSHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115576094T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033473T>A , CM000663.2:g.115033473T>A GRCh38
NC_000001.10:g.115576094T>A , CM000663.1:g.115576094T>A GRCh37
NC_000001.9:g.115377617T>A NCBI36
NG_015891.1:g.8680T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.111T>A MANE Select ENSP00000256592.1:p.Ala37=
ENST00000256592.2:c.111T>A ENSP00000256592.1:p.Ala37=
ENST00000369517.1:c.111T>A ENSP00000358530.1:p.Ala37=
NM_000549.4:c.111T>A NP_000540.2:p.Ala37=
XM_011542065.1:c.111T>A XP_011540367.1:p.Ala37=
XM_011542065.2:c.111T>A XP_011540367.1:p.Ala37=
NM_000549.5:c.111T>A MANE Select NP_000540.2:p.Ala37=
Search 100 bp 5'
Search 100 bp 3'